Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_assertion evidence source_evidence_literature NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_assertion SIO_000772 19412328 NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_assertion wasDerivedFrom befree-20140225 NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_assertion wasGeneratedBy ECO_0000203 NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.